CH EN 5253
Process Design II
Lecture 09
Separations: Distillation Columns and Trains
January 27, 2020
Books
Product and Process Design Principles: Synthesis, Analysis and Evaluation
by J. D Seader, and Warren D. Seider and Daniel R. Lewin,
• Chapter 9
2
Distillation
Distillation Column Internal
4
Plate Types
Bubble Cap Tray Sieve Tray
Packed Towers
• Random Packing
• Structured Packing
Note: Importance of Distributor plate
Equilibrium Equation
• Relative Volatility
• Equilibrium Line
α=KL/KH
Operating and Feed Lines
• Rectifying Section
– R = reflux ratio
– V = vapor flow rate
• Stripping Section
– VB = Boil-up ratio
• Feed Line
Minimum Reflux Ratio
McCabe-Thiele
Step Off Equilibrium Trays
Short cut to Selecting a Column Design
• Minimum Cost for Distillation Column will
occur when you have a
– Minimum of Total Vapor Flow Rate for column
– Occurs at
• R = 1.2 Rmin @ N/Nmin= 2
• Nmin= log[(dLK/bLK)(bHK/dHK)]/log[αLK,HK]
• Rmin ≈ (F/D)/(α-1)
– V = D(R+1)
• V = Vapor Flow Rate
• D = Distillate Flow Rate (Production Rate)
• R = Reflux Ratio
How To Determine the Column Pressure
• Cooling Water Available at 90°F
• Distillate Can be cooled to 120°F min.
• Calculate the Bubble Pt. Pressure of Distillate
Composition at 120°F
– equals Distillate pressure
– Bottoms pressure = Distillate pressure + 10 psia ΔP
• Compute the Bubble Pt. Temp for an estimate of the
Bottoms Composition at Distillate Pressure
– Give Bottoms temperature
• Not Near Critical Point for mixture
Design Issues
• Packing vs Trays
• Column Diameter from flooding consideration
– Relations in Ch 17 of Towler (Design I)
• Column Height
– Relatiopns in Ch 17 of Towler
– N=Nmin/ε (or 2 Nmin/ ε)
• Column Height = N*Htray
• Tray Height = typically 1 ft (or larger)
• Packed Height = Neq*HETP (or 2 Neq*HETP)
– HETP(height equivalent of theoretical plate)
– HETPrandom = 1.5 ft/in*Dp Rule of thumb
• Tray Efficiency, ε = f(viscosityliquid * αLK,HK)
• Pressure Drop
• Tray, ΔP=ρLg hL-wier N
• Packed, ΔP=Packed bed (weeping)
Column Operating Window
• Plate design must ensure good contacting between phases
– Coning: vapor bypasses liquid
– Weeping: liquid drains through to tray below
• Usually design to operate near (~ 70 to 80% of) flooding limits
so as to allow for turn-down
Liquid rate
Vapor
rate
Jet flooding
Downcomer flooding
Weeping
Coning
Excessive
entrainment
Area of satisfactory
operation
Column Costs
• Column – Material of Construction gives ρmetal
– Pressure Vessel Cp= FMCv(W)+CPlatform
– Height may include the reboiler accumulator tank
– Tray Cost = N*Ctray(DT)
– Packing Cost = VpackingCpacking + Cdistributors
• Reboiler CB α AreaHX
• Condenser CB α AreaHX
• Pumping Costs – feed, reflux, reboiler
– Work = Q*ΔP
• Tanks
– Surge tank before column, reboiler accumulator, condensate accumulator
– Pressure Vessel Cp= FMCv(W)+CPlatform
Use of Separation Units
Reaction
Hydrodealkylation of Toluene
Toluene + H2 ⟷ Benzene + CH4
2 Benzene ⟷ Biphenyl + H2
Reactor Effluent
T = 1,350 °F
P = 500 psia
Example
Reactor Effluent
Component kmole/hr
Hydrogen 1292
Methane 1167
Benzene 280
Toluene 117
Biphenyl 3
Total 2859
Reaction Conditions
T = 1,350 °F
P = 500 psia
After Flash to 100F @ 500 psia
Effluent Vapor Liquid
Component kmole/hr kmole/hr kmole/hr
Hydrogen 1292 1290 2
Methane 1167 1149 18
Benzene 280 16 264
Toluene 117 2 115
Biphenyl 3 0 3
Total 2859 2457 402
Recycled Reactants
Further Separation
What separation units should be used?
• Liquid Separation
– Toluene, BP = 111°C
– Benzene, BP = 80°C
– What happens to the Methane (BP = –162 °C) and Biphenyl
(BP = 256°C) impurities?
• Gas Separation
– Hydrogen
– Methane
– What happens to the Toluene and Benzene impurities?
Direct Distillation Sequence
Column Sequences
• Number of Columns
– Nc = P – 1
• P = Number of Products
• No. of Possible Column Sequences
– Ns = [2(P–1)]! / [P!(P–1)!]
• P = Number of Products
P = 3, Nc = 2, Ns = 2
P = 4, Nc = 3, Ns = 5
P = 5, Nc = 4, Ns = 14
P = 6, Nc = 5, Ns = 42
P = 7, Nc = 6, Ns = 132
Number of possible
column sequences
becomes very large
very quickly!
Example
• P = Number of Products = 4 ( A, B, C, D)
• Number of Columns
– Nc = P – 1= 4-1=3
• No. of Possible Column Sequences
– Ns = [2(P–1)]! / [P!(P–1)!]
= [2(4–1)]! / [4!(4–1)!] )
= [2X3]! / [4!X3!]
= 6! / [4!X3!]
= 720 / [24X6]
= 720 / 144
= 5
24
Example
5 Possible Column Sequences
25
Example
How do I evaluate which is the best
sequence of separation columns?
( 1 Problem in HW #4)
26
Example
Marginal Vapor Rate Method
27
Marginal Vapor Rate
• Marginal Annualized Cost Marginal Vapor Rate
• Marginal Annualized Cost proportional to
– Reboiler Duty (Operating Cost)
– Reboiler Area (Capital Cost)
– Condenser Duty (Operating Cost)
– Condenser Area (Capital Cost)
– Diameter of Column (Capital Cost)
• Vapor Rate is proportional to all of the above
~
Selecting Multiple Column Separation Trains
• Minimum Cost for Separation Train will occur
when you have a minimum of Total Vapor
Flow Rate for all columns
R = 1.2 Rmin
V = D(R+1)
V = Vapor Flow Rate
D = Distillate Flow Rate
R = Recycle Ratio
After Quench to 100F @ 500 psia
Effluent Vapor Liquid
Component kmole/hr kmole/hr kmole/hr
Hydrogen 1292 1290 2
Methane 1167 1149 18
Benzene 280 16 264
Toluene 117 2 115
Biphenyl 3 0 3
Total 2859 2457 402
Recycled Reactants
Direct Sequence Indirect Sequence
Distillate Flow Distillate Flow Distillate Flow Distillate Flow
Liquid Column 1 Column 2 Column 1 Column 2
kmole/hr
Hydrogen 2 x x x
Methane 18 x x x
Benzene 264 x x x
Toluene 115 x x
Biphenyl 3
Total 402 284 115 399 284
Sequence Total 399 683
R assumed to be similar for all columns and R > 1
Simplified Marginal Vapor Flow Analysis
(First two columns only)
D=
Separation Train Heuristics
1. Remove thermally unstable, corrosive, or chemically reactive
components early in the sequence.
2. Remove final products one by one as distillates (the direct
sequence).
3. Sequence separation points to remove, early in the sequence, those
components of greatest molar percentage in the feed.
4. Sequence separation points in the order of decreasing relative
volatility so that the most difficult splits are made in the absence of
the other components.
5. Sequence separation points to leave last those separations that give
the highest-purity products.
6. Sequence separation points that favor near equimolar amounts of
distillate and bottoms in each column.

L09-Separations and Column Simulation.pptx

  • 1.
    CH EN 5253 ProcessDesign II Lecture 09 Separations: Distillation Columns and Trains January 27, 2020
  • 2.
    Books Product and ProcessDesign Principles: Synthesis, Analysis and Evaluation by J. D Seader, and Warren D. Seider and Daniel R. Lewin, • Chapter 9 2
  • 3.
  • 4.
  • 5.
    Plate Types Bubble CapTray Sieve Tray
  • 6.
    Packed Towers • RandomPacking • Structured Packing Note: Importance of Distributor plate
  • 7.
    Equilibrium Equation • RelativeVolatility • Equilibrium Line α=KL/KH
  • 8.
    Operating and FeedLines • Rectifying Section – R = reflux ratio – V = vapor flow rate • Stripping Section – VB = Boil-up ratio • Feed Line
  • 9.
  • 10.
  • 11.
  • 12.
    Short cut toSelecting a Column Design • Minimum Cost for Distillation Column will occur when you have a – Minimum of Total Vapor Flow Rate for column – Occurs at • R = 1.2 Rmin @ N/Nmin= 2 • Nmin= log[(dLK/bLK)(bHK/dHK)]/log[αLK,HK] • Rmin ≈ (F/D)/(α-1) – V = D(R+1) • V = Vapor Flow Rate • D = Distillate Flow Rate (Production Rate) • R = Reflux Ratio
  • 13.
    How To Determinethe Column Pressure • Cooling Water Available at 90°F • Distillate Can be cooled to 120°F min. • Calculate the Bubble Pt. Pressure of Distillate Composition at 120°F – equals Distillate pressure – Bottoms pressure = Distillate pressure + 10 psia ΔP • Compute the Bubble Pt. Temp for an estimate of the Bottoms Composition at Distillate Pressure – Give Bottoms temperature • Not Near Critical Point for mixture
  • 14.
    Design Issues • Packingvs Trays • Column Diameter from flooding consideration – Relations in Ch 17 of Towler (Design I) • Column Height – Relatiopns in Ch 17 of Towler – N=Nmin/ε (or 2 Nmin/ ε) • Column Height = N*Htray • Tray Height = typically 1 ft (or larger) • Packed Height = Neq*HETP (or 2 Neq*HETP) – HETP(height equivalent of theoretical plate) – HETPrandom = 1.5 ft/in*Dp Rule of thumb • Tray Efficiency, ε = f(viscosityliquid * αLK,HK) • Pressure Drop • Tray, ΔP=ρLg hL-wier N • Packed, ΔP=Packed bed (weeping)
  • 15.
    Column Operating Window •Plate design must ensure good contacting between phases – Coning: vapor bypasses liquid – Weeping: liquid drains through to tray below • Usually design to operate near (~ 70 to 80% of) flooding limits so as to allow for turn-down Liquid rate Vapor rate Jet flooding Downcomer flooding Weeping Coning Excessive entrainment Area of satisfactory operation
  • 16.
    Column Costs • Column– Material of Construction gives ρmetal – Pressure Vessel Cp= FMCv(W)+CPlatform – Height may include the reboiler accumulator tank – Tray Cost = N*Ctray(DT) – Packing Cost = VpackingCpacking + Cdistributors • Reboiler CB α AreaHX • Condenser CB α AreaHX • Pumping Costs – feed, reflux, reboiler – Work = Q*ΔP • Tanks – Surge tank before column, reboiler accumulator, condensate accumulator – Pressure Vessel Cp= FMCv(W)+CPlatform
  • 17.
  • 18.
    Reaction Hydrodealkylation of Toluene Toluene+ H2 ⟷ Benzene + CH4 2 Benzene ⟷ Biphenyl + H2 Reactor Effluent T = 1,350 °F P = 500 psia Example
  • 19.
    Reactor Effluent Component kmole/hr Hydrogen1292 Methane 1167 Benzene 280 Toluene 117 Biphenyl 3 Total 2859 Reaction Conditions T = 1,350 °F P = 500 psia
  • 20.
    After Flash to100F @ 500 psia Effluent Vapor Liquid Component kmole/hr kmole/hr kmole/hr Hydrogen 1292 1290 2 Methane 1167 1149 18 Benzene 280 16 264 Toluene 117 2 115 Biphenyl 3 0 3 Total 2859 2457 402 Recycled Reactants
  • 21.
    Further Separation What separationunits should be used? • Liquid Separation – Toluene, BP = 111°C – Benzene, BP = 80°C – What happens to the Methane (BP = –162 °C) and Biphenyl (BP = 256°C) impurities? • Gas Separation – Hydrogen – Methane – What happens to the Toluene and Benzene impurities?
  • 22.
  • 23.
    Column Sequences • Numberof Columns – Nc = P – 1 • P = Number of Products • No. of Possible Column Sequences – Ns = [2(P–1)]! / [P!(P–1)!] • P = Number of Products P = 3, Nc = 2, Ns = 2 P = 4, Nc = 3, Ns = 5 P = 5, Nc = 4, Ns = 14 P = 6, Nc = 5, Ns = 42 P = 7, Nc = 6, Ns = 132 Number of possible column sequences becomes very large very quickly!
  • 24.
    Example • P =Number of Products = 4 ( A, B, C, D) • Number of Columns – Nc = P – 1= 4-1=3 • No. of Possible Column Sequences – Ns = [2(P–1)]! / [P!(P–1)!] = [2(4–1)]! / [4!(4–1)!] ) = [2X3]! / [4!X3!] = 6! / [4!X3!] = 720 / [24X6] = 720 / 144 = 5 24
  • 25.
  • 26.
    Example How do Ievaluate which is the best sequence of separation columns? ( 1 Problem in HW #4) 26
  • 27.
  • 28.
    Marginal Vapor Rate •Marginal Annualized Cost Marginal Vapor Rate • Marginal Annualized Cost proportional to – Reboiler Duty (Operating Cost) – Reboiler Area (Capital Cost) – Condenser Duty (Operating Cost) – Condenser Area (Capital Cost) – Diameter of Column (Capital Cost) • Vapor Rate is proportional to all of the above ~
  • 29.
    Selecting Multiple ColumnSeparation Trains • Minimum Cost for Separation Train will occur when you have a minimum of Total Vapor Flow Rate for all columns R = 1.2 Rmin V = D(R+1) V = Vapor Flow Rate D = Distillate Flow Rate R = Recycle Ratio
  • 30.
    After Quench to100F @ 500 psia Effluent Vapor Liquid Component kmole/hr kmole/hr kmole/hr Hydrogen 1292 1290 2 Methane 1167 1149 18 Benzene 280 16 264 Toluene 117 2 115 Biphenyl 3 0 3 Total 2859 2457 402 Recycled Reactants
  • 31.
    Direct Sequence IndirectSequence Distillate Flow Distillate Flow Distillate Flow Distillate Flow Liquid Column 1 Column 2 Column 1 Column 2 kmole/hr Hydrogen 2 x x x Methane 18 x x x Benzene 264 x x x Toluene 115 x x Biphenyl 3 Total 402 284 115 399 284 Sequence Total 399 683 R assumed to be similar for all columns and R > 1 Simplified Marginal Vapor Flow Analysis (First two columns only) D=
  • 32.
    Separation Train Heuristics 1.Remove thermally unstable, corrosive, or chemically reactive components early in the sequence. 2. Remove final products one by one as distillates (the direct sequence). 3. Sequence separation points to remove, early in the sequence, those components of greatest molar percentage in the feed. 4. Sequence separation points in the order of decreasing relative volatility so that the most difficult splits are made in the absence of the other components. 5. Sequence separation points to leave last those separations that give the highest-purity products. 6. Sequence separation points that favor near equimolar amounts of distillate and bottoms in each column.